Crushing behavior of alumina inclusions with different porosity during hot compression

Alumina inclusions in commercial as-cast 2.25Cr1Mo0.25V aluminum deoxidized steel exhibited a feature of porous structure. In order to investigate the crushing characteristics of alumina inclusion during hot working, a series of alumina blocks with different porosity whose properties are similar to the alumina inclusions in ingots were prepared using spark plasma sintering. The crushing behavior of alumina blocks during hot compression with quasi-static load was studied. A prediction model of compressive strength of alumina inclusions considering apparent porosity was established on basis of hyperbolic sine Arrhenius equation. A novel crushing mode diagram for alumina inclusions characterized by Z parameter was proposed. The crushing mechanism of alumina inclusions under different deformation parameters was clarified by fracture characteristics. The results showed that the hot compression process of alumina presented a typical brittle fracture, the compressive strength was more sensitive to deformation conditions at lower apparent porosity as compared with the conditions of higher apparent porosity. With the increase of Z, the crushing mode of alumina inclusions gradually changed from intergranular fracture to transgranular fracture.     

A selective organosilica membrane for ethyl acetate dehydration by pervaporation

Organosilica bis(triethoxysilyl) ethane (BTESE) membranes were explored for pervaporation dehydration of binary and ternary mixtures of ethyl acetate (EA) by undiluted sol coating combined with flash firing. Three BTESE membranes (M1, M2, and M3) were fabricated on macroporous supports by varying BTESE concentrations (0.5, 2.5, and 5 wt% BTESE, respectively) in polymer sols. The membranes were characterized by DLS, SEM, FTIR, XRD, contact angle, AFM, and pervaporation performance to discuss the effect of the BTESE contents in the polymer sol on the formation and dehydration performance of resulting organosilica membranes. It was found that 5 wt% loading of BTESE led to a highly selective membrane for dehydration of EA/H₂O mixture. Among the synthesized membranes, M3 delivered flux of 0.84 ± 0.05 kg.m⁻².h⁻¹ with a selectivity of >10,000 for EA/H₂O mixture (98/2 wt%) at 60°C. The time course of pervaporation dehydration for the EA/H₂O mixture (95/5 wt%) confirms the stability of BTESE membrane in the investigated time period of 120 h. Further, the membrane exhibited excellent selectivity larger than 10,000 for separation of ternary mixtures (90/2/8 wt%) of ethyl acetate/ethanol/water and n-propyl acetate/isopropanol/water respectively, the composition of which is similar to the top product of the distillation column used in the industrial esterification process. The best separation performance and excellent acid stability of BTESE membranes in this study suggest that the simple synthesis protocol of undiluted sol coating and flash firing will provide a cost-effective, quick, and efficient synthesis route for practical membrane based applications.     

Inhibiting effect of heterogeneous cations aggregation enhanced by oxygen deficiency on glass formation of BaTi2O5 melts

Although remarkable development of titanate-based glasses has been achieved, challenge remains to elucidate the correlation between structure and glass-forming properties in these systems due to their complex structure that is inconsistent with the classic Zachariasen's model. In this work, we aim to correlate the structural evolution of titanate melts to their glass-forming ability (GFA). The prototypical material barium dititanate (BaTi₂O₅, BT2) melts with different GFA were rendered by controlled melting atmospheres, and the corresponding structural changes were determined using in situ high-energy synchrotron X-ray diffraction combined with empirical potential structure refinement and ab initio molecular dynamics. The results show that BT2 melt in reducing atmosphere shows poor GFA but that in oxidizing atmosphere presents good GFA. Structural analysis demonstrates the mean coordination number of [TiO_m] polyhedra is analogous in the melt under two different atmospheres but an enhanced heterogeneous cations aggregation takes place in the melt under reducing atmosphere, which is closely related to oxygen-deficiencies. Furthermore, we reveal that the enhanced heterogeneous cations aggregation promotes crystallization (and therefore hinders glass formation) through disordering the distribution of [TiO_m] and [BaO_n] polyhedra, changing the connectivity between these polyhedra, creating more crystal-like Ti-Ti clusters, and decreasing topological disorder of BT2 melt. Our work provides a new viewpoint to understand the GFA of titanates melt from structural heterogeneity beyond the previous perspectives that only focus on [TiO_m] polyhedra.     

Porous nitrogen-enriched hollow carbon nanofibers as freestanding electrode for enhanced lithium storage

One-dimensional porous carbons bearing high surface areas and sufficient heteroatom doped functional-ities are essential for advanced electrochemical energy storage devices, especially for developing free-standing film electrodes. Here we develop a porous, nitrogen-enriched, freestanding hollow carbon nanofiber (PN-FHCF) electrode material via filtration of polypyrrole (PPy) hollow nanofibers formed by in situ self-degraded template-assisted strategy, followed by NH3-assisted carbonization. The PN-FHCF retains the freestanding film morphology that is composed of three-dimensional networks from the entanglement of 1D nanofiber and delivers 3.7-fold increase in specific surface area (592 m2·g-1) com-pared to the carbon without NH3 treatment (FHCF). In spite of the enhanced specific surface area, PN-FHCF still exhibits comparable high content of surface N functionalities (8.8％, atom fraction) to FHCF. Such developed hierarchical porous structure without sacrificing N doping functionalities together enables the achievement of high capacity, high-rate property and good cycling stability when applied as self-supporting anode in lithium-ion batteries, superior to those of FHCF without NH3 treatment.     

Real-time molecular characterization of air pollutants in a Hong Kong residence: Implication of indoor source emissions and heterogeneous chemistry

Due to the high health risks associated with indoor air pollutants and long-term exposure, indoor air quality has received increasing attention. In this study, we put emphasis on the molecular composition, source emissions, and chemical aging of air pollutants in a residence with designed activities mimicking ordinary Hong Kong homes. More than 150 air pollutants were detected at molecular level, 87 of which were quantified at a time resolution of not less than 1 hour. The indoor-to-outdoor ratios were higher than 1 for most of the primary air pollutants, due to emissions of indoor activities and indoor backgrounds (especially for aldehydes). In contrast, many secondary air pollutants exhibited higher concentrations in outdoor air. Painting ranked first in aldehyde emissions, which also caused great enhancement of aromatics. Incense burning had the highest emissions of particle-phase organics, with vanillic acid and syringic acid as markers. The other noteworthy fingerprints enabled by online measurements included linoleic acid, cholesterol, and oleic acid for cooking, 2,5-dimethylfuran, stigmasterol, iso-/anteiso-alkanes, and fructose isomers for smoking, C₂₈-C₃₄ even n-alkanes for candle burning, and monoterpenes for the use of air freshener, cleaning agents, and camphor oil. We showed clear evidence of chemical aging of cooking emissions, giving a hint of indoor heterogeneous chemistry. This study highlights the value of organic molecules measured at high time resolutions in enhancing our knowledge on indoor air quality.     

Indoor solid fuel use for heating and cooking with blood pressure and hypertension: A cross-sectional study among middle-aged and older adults in China

A cross-sectional study was conducted to investigate the impact of solid fuel use for heating and cooking on blood pressure (BP) and hypertension, using data from the China Health and Retirement Longitudinal Study (CHARLS). The primary fuels used for indoor heating and cooking were collected by questionnaires, respectively. Hypertension was defined based on self-report of physician's diagnosis, and/or measured BP, and/or anti-hypertensive medication use. Multivariate logistic regression models were constructed to assess the associations. Among 10 450 eligible participants, 68.2% and 57.2% used indoor solid fuel for heating and cooking, respectively. Compared with none/clean fuel users, solid fuel for heating was associated with elevated BP (adjusted β: 2.02, 95% CI: 1.04–3.01 for systolic BP; adjusted β: 1.36, 95% CI: 0.78–1.94 for diastolic BP) and increased risk of hypertension (adjusted odds ratio: 1.15, 95% CI: 1.03–1.29). The impact of indoor solid fuel for heating on BP was more evident in rural and north residents, and hypertensive patients. We did not detect any significant associations between solid fuel use for cooking and BP/hypertension. Indoor solid fuel use is prevalent in China, especially in the rural areas. Its negative impact on BP suggested that modernization of household fuel use may help to reduce the burden of hypertension in China.     

Effect of RF magnetron sputtering parameters on the optimization of the discharge capacity of ternary lithium oxide thin films

Journal of Materials Science: Materials in Electronics - The increasing demand for lithium-ion batteries has stimulated the investigation of new compounds in order to reduce the costs and the...     

Contributions of oxygen vacancies to the hydrogen evolution catalytic activity of tungsten oxides

The tungsten trioxide attracts less attention due to the low electron transfer kinetics that hinders the interaction of electrons and ions during the hydrogen evolution reaction (HER). But the oxygen vacancy strategy can inspire its electrocatalytic activity for HER because it has a positive effect on improving the charge transfer and compensating for the weak hydrogen adsorption of the tungsten trioxide. By synthesizing a series of substoichiometric tungsten oxides, we reveal the linear relationship between the catalytic activity and the content of oxygen vacancies, which indicates that the oxygen vacancy strategy is an achievable route to enhance the HER for metal oxides.